anxiety of pain

Assessment the effect of desensitization method with eye movements and reprocessing on anxiety induced by dressing pain in burn patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014060117937N1

Enrollment

Registered

2014-09-03

Start date

2014-03-04

Completion date

Unknown

Last updated

2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn patients. Burns and corrosions

Interventions

Intervention 1: Patients in intervention group should do the followings with the guidance and cooperation of therapist. The visual embodiment of an image most prominent of the traumatic scene. Focusin

Patients in intervention group should do the followings with the guidance and cooperation of therapist. The visual embodiment of an image most prominent of the traumatic scene. Focusing on the negat

Control group: the group that will receive the standard treatment ordered by the physician according to the hospital protocol by staff and the interventions will not be performed by the researcher.

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Grade 2 burn which diagnosed by specialist physician? Patients have passed the acute phase of illness? Patients didn’t have a history of seizures? The level of education should be higher than fifth grade? Patients didn’t have a history of mental illness? Patients who dont have drug addiction? Patients were between 18 and 60 years old? Patients shouldn’t have strabismus or vision problems? Patients should be able to speak and understand Persian language? Patients shouldn’t have burns on head, face and respiratory system? Patients experienced dressing change at least once after their admission. Exclusion criteria: Patients are not able to tolerate the treatment method? Patients don’t cooperate with the therapist? Patients who candidate for skin graft surgery after choose.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Anxiety of burn pain. Timepoint: Ninety-six days simultaneously in the intervention and control groups. Method of measurement: Burns Specific Pain Anxiety Scale.	—

Secondary

Measure	Time frame
Outcome of patient care. Timepoint: Ninety-six days simultaneously in the intervention and control groups. Method of measurement: Burns Specific Pain Anxiety Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMostafa chatrrooz

Qazvin University of Medical Sciences

mchatrrooz@qums.ac.ir+98 28 3333 8127

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026